Fluoro(phenylthio)acetonitrile
≥97%(GC)
- Product Code: 81678
CAS:
130612-84-9
| Molecular Weight: | 167.20 g./mol | Molecular Formula: | C₈H₆FNS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797105 | |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
Fluoro(phenylthio)acetonitrile is primarily used as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its unique structure, featuring both a fluoro and phenylthio group, allows it to participate in various chemical reactions, such as nucleophilic substitutions and cyclizations, making it valuable for constructing complex molecules. In medicinal chemistry, it is employed to develop compounds with potential biological activity, including antimicrobial and anticancer agents. Additionally, its reactivity is leveraged in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. The compound's ability to introduce fluorine atoms into organic molecules is particularly advantageous, as fluorinated compounds often exhibit enhanced stability, bioavailability, and metabolic resistance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $77.77 |
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Fluoro(phenylthio)acetonitrile
Fluoro(phenylthio)acetonitrile is primarily used as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its unique structure, featuring both a fluoro and phenylthio group, allows it to participate in various chemical reactions, such as nucleophilic substitutions and cyclizations, making it valuable for constructing complex molecules. In medicinal chemistry, it is employed to develop compounds with potential biological activity, including antimicrobial and anticancer agents. Additionally, its reactivity is leveraged in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. The compound's ability to introduce fluorine atoms into organic molecules is particularly advantageous, as fluorinated compounds often exhibit enhanced stability, bioavailability, and metabolic resistance.
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